Canonical Allele Identifier: CA418818851

Gene: ABCA4

Linked Data

• MyVariant Identifiers: chr1:g.94522310G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94056754G>T , CM000663.2:g.94056754G>T	GRCh38
NC_000001.10:g.94522310G>T , CM000663.1:g.94522310G>T	GRCh37
NC_000001.9:g.94294898G>T	NCBI36
NG_009073.1:g.69396C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370225.4:c.2229C>A MANE Select	ENSP00000359245.3:p.Ala743=
ENST00000649773.1:c.2161-1439C>A	ENSP00000496882.1:n.2161-1439C>A
ENST00000370225.3:c.2229C>A	ENSP00000359245.3:p.Ala743=
ENST00000536513.5:c.-65+6420C>A	ENSP00000439707.2:n.-65+6420C>A
NM_000350.2:c.2229C>A	NP_000341.2:p.Ala743=
NM_000350.3:c.2229C>A MANE Select	NP_000341.2:p.Ala743=